반응 #54296

ord-87e20e5127b94517aacddcda20ba5ec1

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONTo a suspension of 12.21 g
  2. 2
    workup.STIRRINGthe mixture stirred an additional 1/2 hour
  3. 3
    workup.ADDITIONTo the solution is added a solution of 9.88 g
  4. 4
    workup.STIRRINGAfter stirring for 24 hours
  5. 5
    기타the THF is removed in vacuo
  6. 6
    기타the residue partitioned with chloroform/water
  7. 7
    기타The oily residue is triturated with 300 ml
  8. 8
    기타benzene to give a white solid
  9. 9
    workup.DISSOLUTIONThis is dissolved in 50 ml
  10. 10
    온도cooled
  11. 11
    여과The white solid which forms is filtered
  12. 12
    기타air dried

실험 절차

To a suspension of 12.21 g. (0.05 moles) of methyl guanidine sulfate in 110 ml. of tetrahydrofuran is added 8.0 g. (0.10 moles of sodium hydroxide) of 50% aqueous sodium hydroxide. After stirring for 11/2 hours, 4.5 g. of sodium sulfate is slowly added and the mixture stirred an additional 1/2 hour. To the solution is added a solution of 9.88 g. (0.05 moles) of 2,6-dimethylphenyl-N-methylcarbamoyl chloride in 30 ml. of tetrahydrofuran. After stirring for 24 hours, the THF is removed in vacuo and the residue partitioned with chloroform/water. The oily residue is triturated with 300 ml. of hexane and 20 ml. benzene to give a white solid. This is dissolved in 50 ml. of 1:4 HNO3 and warmed slightly over 1/2 hour, then cooled. The white solid which forms is filtered and air dried to obtain 1-(2',6'-dimethylphenyl)-1-methyl-3-methylamidinourea nitrate.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04147804uspto-grants-1979_04